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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 5
2003 8
2004 5
2005 5
2006 5
2007 8
2008 5
2009 9
2010 10
2011 4
2012 8
2013 3
2014 7
2015 5
2016 18
2017 10
2018 7
2019 8
2020 2
2021 2
2022 3
2023 3
2024 1

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122 results

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Page 1
Nosology of genetic skeletal disorders: 2023 revision.
Unger S, Ferreira CR, Mortier GR, Ali H, Bertola DR, Calder A, Cohn DH, Cormier-Daire V, Girisha KM, Hall C, Krakow D, Makitie O, Mundlos S, Nishimura G, Robertson SP, Savarirayan R, Sillence D, Simon M, Sutton VR, Warman ML, Superti-Furga A. Unger S, et al. Among authors: cohn dh. Am J Med Genet A. 2023 May;191(5):1164-1209. doi: 10.1002/ajmg.a.63132. Epub 2023 Feb 13. Am J Med Genet A. 2023. PMID: 36779427
Nosology and classification of genetic skeletal disorders: 2019 revision.
Mortier GR, Cohn DH, Cormier-Daire V, Hall C, Krakow D, Mundlos S, Nishimura G, Robertson S, Sangiorgi L, Savarirayan R, Sillence D, Superti-Furga A, Unger S, Warman ML. Mortier GR, et al. Among authors: cohn dh. Am J Med Genet A. 2019 Dec;179(12):2393-2419. doi: 10.1002/ajmg.a.61366. Epub 2019 Oct 21. Am J Med Genet A. 2019. PMID: 31633310
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies.
Zhang W, Taylor SP, Ennis HA, Forlenza KN, Duran I, Li B, Sanchez JAO, Nevarez L, Nickerson DA, Bamshad M; University of Washington Center for Mendelian Genomics; Lachman RS, Krakow D, Cohn DH. Zhang W, et al. Among authors: cohn dh. Hum Mutat. 2018 Jan;39(1):152-166. doi: 10.1002/humu.23362. Epub 2017 Nov 6. Hum Mutat. 2018. PMID: 29068549 Free PMC article.
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.
Marini JC, Forlino A, Cabral WA, Barnes AM, San Antonio JD, Milgrom S, Hyland JC, Körkkö J, Prockop DJ, De Paepe A, Coucke P, Symoens S, Glorieux FH, Roughley PJ, Lund AM, Kuurila-Svahn K, Hartikka H, Cohn DH, Krakow D, Mottes M, Schwarze U, Chen D, Yang K, Kuslich C, Troendle J, Dalgleish R, Byers PH. Marini JC, et al. Among authors: cohn dh. Hum Mutat. 2007 Mar;28(3):209-21. doi: 10.1002/humu.20429. Hum Mutat. 2007. PMID: 17078022 Free PMC article. Review.
In Situ Generated Medical Devices.
Cohn D, Sloutski A, Elyashiv A, Varma VB, Ramanujan R. Cohn D, et al. Adv Healthc Mater. 2019 Apr;8(8):e1801066. doi: 10.1002/adhm.201801066. Epub 2019 Mar 4. Adv Healthc Mater. 2019. PMID: 30828989 Review.
Engineering In Situ Weldable Vascular Devices.
Cohn D, Widlan F, Zarek M, Peselev Z, Bloom AI. Cohn D, et al. Bioengineering (Basel). 2023 Feb 7;10(2):221. doi: 10.3390/bioengineering10020221. Bioengineering (Basel). 2023. PMID: 36829715 Free PMC article.
Dominant-negative SOX9 mutations in campomelic dysplasia.
Csukasi F, Duran I, Zhang W, Martin JH, Barad M, Bamshad M, Weis MA, Eyre D, Krakow D, Cohn DH. Csukasi F, et al. Among authors: cohn dh. Hum Mutat. 2019 Dec;40(12):2344-2352. doi: 10.1002/humu.23888. Epub 2019 Aug 26. Hum Mutat. 2019. PMID: 31389106 Free PMC article.
Gender and neglected tropical disease front-line workers: Data from 16 countries.
Shoemaker EA, Dale K, Cohn DA, Kelly MP, Zoerhoff KL, Batcho WE, Bougouma C, Nko'Ayissi GB, Meite A, Marfo B, Goepogui A, Telfort MA, Sianipar LR, Traore M, Rimal P, Alfari DA, Anyaike C, Badiane FN, Kargbo-Labour I, Mwingira UJ, Awoussi MS, Stelmach RD, Smith CL, Arney J, Faramand TH, Stukel DM, Pou B, Rotondo LA, Kraemer JD, Baker MC. Shoemaker EA, et al. Among authors: cohn da. PLoS One. 2019 Dec 19;14(12):e0224925. doi: 10.1371/journal.pone.0224925. eCollection 2019. PLoS One. 2019. PMID: 31856174 Free PMC article. Review.
The skeletal dysplasias: clinical-molecular correlations.
Rimoin DL, Cohn D, Krakow D, Wilcox W, Lachman RS, Alanay Y. Rimoin DL, et al. Among authors: cohn d. Ann N Y Acad Sci. 2007 Nov;1117:302-9. doi: 10.1196/annals.1402.072. Ann N Y Acad Sci. 2007. PMID: 18056050 Review.
122 results